Canonical Allele Identifier: CA366234996

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2790168
• ClinVar RCV Id: RCV003669712
• MyVariant Identifiers: chr6:g.157511213G>C (hg19) ; chr6:g.157190079G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190079G>C , CM000668.2:g.157190079G>C	GRCh38
NC_000006.11:g.157511213G>C , CM000668.1:g.157511213G>C	GRCh37
NC_000006.10:g.157552905G>C	NCBI36
NG_032093.1:g.417150G>C
NG_032093.2:g.417150G>C
NG_066624.1:g.419054G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3941G>C	ENSP00000055163.8:p.Ser1314Thr
ENST00000414678.8:c.4010G>C	ENSP00000412835.3:p.Ser1337Thr
ENST00000637015.2:c.4229G>C	ENSP00000489729.2:p.Ser1410Thr
ENST00000346085.10:c.3980G>C	ENSP00000344546.5:p.Ser1327Thr
ENST00000350026.10:c.3692G>C	ENSP00000055163.7:p.Ser1231Thr
ENST00000414678.7:c.2258G>C	ENSP00000412835.2:p.Ser753Thr
ENST00000635849.1:c.1421G>C	ENSP00000490948.1:p.Ser474Thr
ENST00000635957.1:c.1052G>C	ENSP00000490385.1:p.Ser351Thr
ENST00000636930.2:c.4100G>C MANE Select	ENSP00000490491.2:p.Ser1367Thr
ENST00000636940.1:n.2097G>C
ENST00000637015.1:c.1468G>C
ENST00000637568.1:c.1382G>C
ENST00000637741.1:n.766G>C
ENST00000637810.1:c.1442G>C	ENSP00000489636.1:p.Ser481Thr
ENST00000637904.1:c.1601G>C	ENSP00000490550.1:p.Ser534Thr
ENST00000647938.1:c.3731G>C	ENSP00000498155.1:p.Ser1244Thr
ENST00000346085.9:c.3731G>C	ENSP00000344546.4:p.Ser1244Thr
ENST00000350026.9:c.3692G>C	ENSP00000055163.7:p.Ser1231Thr
ENST00000414678.6:c.2258G>C	ENSP00000412835.2:p.Ser753Thr
NM_017519.2:c.3692G>C	NP_059989.2:p.Ser1231Thr
NM_020732.3:c.3731G>C	NP_065783.3:p.Ser1244Thr
XM_005267069.3:c.3851G>C	XP_005267126.2:p.Ser1284Thr
XM_011535984.1:c.2930G>C	XP_011534286.1:p.Ser977Thr
XM_011535985.1:c.2750G>C	XP_011534287.1:p.Ser917Thr
XM_011535986.1:c.2510G>C	XP_011534288.1:p.Ser837Thr
XM_011535987.1:c.2129G>C	XP_011534289.1:p.Ser710Thr
XM_011535988.1:c.992G>C	XP_011534290.1:p.Ser331Thr
NM_001346813.1:c.3851G>C	NP_001333742.1:p.Ser1284Thr
NM_001363725.1:c.1601G>C	NP_001350654.1:p.Ser534Thr
XM_011535984.2:c.4061G>C	XP_011534286.2:p.Ser1354Thr
XM_011535988.3:c.992G>C	XP_011534290.1:p.Ser331Thr
XM_017011103.2:c.3962G>C	XP_016866592.1:p.Ser1321Thr
XM_017011104.1:c.3932G>C	XP_016866593.1:p.Ser1311Thr
XM_017011105.2:c.3902G>C	XP_016866594.1:p.Ser1301Thr
XM_017011106.2:c.3773G>C	XP_016866595.1:p.Ser1258Thr
XM_017011107.2:c.3752G>C	XP_016866596.1:p.Ser1251Thr
XR_002956289.1:n.4144G>C
NM_001363725.2:c.1601G>C	NP_001350654.1:p.Ser534Thr
NM_001371656.1:c.3980G>C	NP_001358585.1:p.Ser1327Thr
NM_001374820.1:c.3980G>C	NP_001361749.1:p.Ser1327Thr
NM_001374828.1:c.4100G>C MANE Select	NP_001361757.1:p.Ser1367Thr
NM_017519.3:c.3941G>C	NP_059989.3:p.Ser1314Thr